statistiche ricercatore

Continente	#
NA - Nord America	681
AS - Asia	528
EU - Europa	485
SA - Sud America	64
Continente sconosciuto - Info sul continente non disponibili	30
AF - Africa	11
Totale	1.799

Nazione	#
US - Stati Uniti d'America	653
SG - Singapore	192
RU - Federazione Russa	187
IT - Italia	165
VN - Vietnam	142
CN - Cina	100
BR - Brasile	48
DE - Germania	34
HK - Hong Kong	32
FR - Francia	27
NL - Olanda	19
CA - Canada	17
IN - India	17
GB - Regno Unito	12
FI - Finlandia	11
PH - Filippine	9
PL - Polonia	8
AR - Argentina	7
BD - Bangladesh	6
IE - Irlanda	5
JP - Giappone	5
MX - Messico	5
UA - Ucraina	5
EC - Ecuador	4
IQ - Iraq	4
TH - Thailandia	4
CI - Costa d'Avorio	3
CO - Colombia	3
ES - Italia	3
PA - Panama	3
PK - Pakistan	3
SE - Svezia	3
CL - Cile	2
JO - Giordania	2
KR - Corea	2
ZA - Sudafrica	2
AT - Austria	1
BE - Belgio	1
BG - Bulgaria	1
BS - Bahamas	1
BW - Botswana	1
BY - Bielorussia	1
CY - Cipro	1
GA - Gabon	1
GH - Ghana	1
HT - Haiti	1
HU - Ungheria	1
ID - Indonesia	1
IR - Iran	1
KH - Cambogia	1
KZ - Kazakistan	1
LT - Lituania	1
MR - Mauritania	1
MY - Malesia	1
NA - Namibia	1
OM - Oman	1
PS - Palestinian Territory	1
SV - El Salvador	1
TR - Turchia	1
TW - Taiwan	1
XK - ???statistics.table.value.countryCode.XK???	1
YT - Mayotte	1
Totale	1.770

Nome	#
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells	216
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses	190
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency	178
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation	172
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features	160
Targeting mitochondrial network architecture in down syndrome and aging	159
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs	155
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells	143
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome	143
Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother	142
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report	141
Totale	1.799

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	88	0	0	0	1	5	3	0	9	13	7	28	22
2022/2023	140	13	9	10	11	13	14	4	18	27	14	4	3
2023/2024	72	1	16	2	4	2	12	2	8	0	3	15	7
2024/2025	384	27	5	5	4	12	12	29	40	19	43	149	39
2025/2026	861	92	59	79	94	168	37	111	28	117	49	24	3
2026/2027	108	9	24	45	30	0	0	0	0	0	0	0	0
Totale													1.799